HRID426379

反应详情

EQUATION

反应方程式

HRID 426379 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

24.3 g (100 mmol) of 9-phenylcarbazole was put into a 2 L Meyer flask, and dissolved in 600 mL of glacial acetic acid. Then, 17.8 g (100 mmol) of N-bromosuccinimide was slowly added, and the solution was stirred for about 12 hours at room temperature. This solution was dropped into 1 L of ice water while stirring. A white solid precipitated was collected by suction filtration, and then washed with water three times. This solid was dissolved in 150 mL of diethyl ether, and the solution was washed with a saturated aqueous solution of sodium bicarbonate and then with water. The organic layer was dried over magnesium sulfate, filtered, and concentrated, and then the residue was dissolved in ca. 50 mL of ethanol. The precipitate formed as a white solid was collected by suction filtration and dried, giving 28.4 g (88% yield) of 3-bromo-9-phenylcarbazole as white powder.

WORKUP

后处理

  1. stirringwhile stirring
  2. customA white solid precipitated
  3. filtrationwas collected by suction filtration
  4. washwashed with water three times
  5. dissolutionThis solid was dissolved in 150 mL of diethyl ether
  6. washthe solution was washed with a saturated aqueous solution of sodium bicarbonate
  7. dry with materialThe organic layer was dried over magnesium sulfate
  8. filtrationfiltered
  9. concentrationconcentrated
  10. dissolutionthe residue was dissolved in ca. 50 mL of ethanol
  11. customThe precipitate formed as a white solid
  12. filtrationwas collected by suction filtration
  13. customdried